Register a trial

The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT05408572




Registration number
NCT05408572
Ethics application status
Date submitted
1/06/2022
Date registered
7/06/2022

Titles & IDs
Public title
Study of SON-1010 (IL12-FHAB) in Healthy Adults
Scientific title
A Phase 1, Randomized, Adaptive-Design, Dose-Escalation Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of SON-1010 (IL12-FHAB) in Healthy Adults
Secondary ID [1] 0 0
SB102
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Healthy Adult 0 0
Condition category
Condition code

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Other - SON-1010 (IL12-FHAB)

Experimental: Single Dose Level 1 - 6 healthy adults dosed with SON-1010 (Level 1) + 2 healthy adults dosed with Placebo

Experimental: Single Dose Level 2 - 6 healthy adults dosed with SON-1010 (Level 2) + 2 healthy adults dosed with Placebo

Experimental: Single Dose Level 3 - 6 healthy adults dosed with SON-1010 (Level 3) + 2 healthy adults dosed with Placebo

Experimental: Single Dose Level 4 - 6 healthy adults dosed with SON-1010 (Level 4) + 2 healthy adults dosed with Placebo

Experimental: Single Dose Level 5 - 6 healthy adults dosed with SON-1010 (Level 5) + 2 healthy adults dosed with Placebo


Treatment: Other: SON-1010 (IL12-FHAB)
SON-1010 is a single-chain human IL-12 cytokine linked to a single-chain variable region known as the FHAB.
Intervention code [1] 0 0
Treatment: Other
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
To evaluate the safety and tolerability of SON-1010 as a single-ascending dose (SAD) in healthy adults.
Timepoint [1] 0 0
Study Duration - Week 1 on Day 1, 2, 3 ,4, 5. Follow-Up on Day 8, 10, 12, 15, 22, 29
Secondary outcome [1] 0 0
Serum and urine concentrations of SON-1010 will be determined at various time points
Timepoint [1] 0 0
Study Duration - Week 1 on Day 1, 2, 3 ,4, 5. Follow-Up on Day 8, 10, 12, 15, 22, 29
Secondary outcome [2] 0 0
Effect of SON-1010 on Serum cytokine levels
Timepoint [2] 0 0
Study Duration - Week 1 on Day 1, 2, 3 ,4, 5. Follow-Up on Day 8, 10, 12, 15, 22, 29
Secondary outcome [3] 0 0
Evaluation of SON-1010 immunogenicity
Timepoint [3] 0 0
Study Duration - Week 1 on Day 1, 2, 3 ,4, 5. Follow-Up on Day 8, 10, 12, 15, 22, 29

Eligibility
Key inclusion criteria
Inclusion Criteria

* Participants must be medically healthy based on medical history, physical examination, and clinical laboratory testing.
* Participants must be between 18 to 54 years of age, inclusive at the time of the informed consent.
* May only be limited users of nicotine-containing products, including e-cigarettes, for at least 3 continuous months before the first dose of SON-1010, as confirmed by cotinine testing at screening and check-in (day -1). Social smoking is allowed up to 5 cigarettes per week as long as the participant is willing to abstain during confinement and the cotinine test is negative at check in. One repeat test is permitted at screening.
* Must have negative drug/alcohol testing at screening and check-in (day -1). Screening drug/alcohol testing may be repeated once if deemed appropriate.
* Must have vital signs (after sitting for at least 5 minutes) within the following ranges at screening and check-in (day -1):

* Systolic blood pressure (BP), 90 to 140 mmHg, inclusive
* Diastolic BP, 40 to 90 mmHg, inclusive
* Heart rate (HR) >50 to =100 beats per minute
* Must weigh >50 kg and =100 kg and have body mass index (BMI) =18 and =32 kg/m2 at screening.
* Must have normal laboratory function by day -1 (note that the screening safety laboratory assessment may be repeated once to confirm the initial result and trending), defined as:

* Creatinine level = upper limit of normal (ULN) for age
* Alanine aminotransferase (ALT) = ULN
* Total bilirubin = ULN (unless participant has Grade 1 bilirubin elevation due to Gilbert's disease or a similar syndrome involving slow conjugation of bilirubin and direct bilirubin is <35%)
* Albumin > lower limit of normal (LLN)
* Coagulation International Normalized Ratio (INR) < 1.5
* Females of childbearing potential, <1-year postmenopause who are not permanently sterile, must have a negative serum pregnancy test (beta-human chorionic gonadotropin [ß-HCG]) at day -1, and agree to abstinence or use 2 highly effective methods of birth control for 30 days before the study, during the study, and for 30 days after the last dose of study intervention. Females who are not of childbearing potential (have had a hysterectomy, bilateral oophorectomy, or are = 1-year postmenopause) do not need to use any contraception Nonchildbearing potential is defined as surgically sterile or postmenopausal (defined as 12 months of spontaneous amenorrhea). A follicle stimulating hormone (FSH) level >40 IU/L at screening will confirm postmenopausal status. If a participant is not sexually active, but becomes active, then she and her male partner must use 2 methods of adequate contraception.
* Males and their female partners must use a highly effective method of birth control if female partner(s) is of childbearing potential and must not donate sperm during the study and for 90 days after the last dose of study intervention. Contraception guidance is described in the protocol.
* Willing and able to provide signed informed consent as described in the protocol which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.
* Must be able to communicate well with Investigator and/or study site personnel and to comply with the requirements of the entire study.
Minimum age
18 Years
Maximum age
54 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
Exclusion Criteria

* Concurrent conditions that could interfere with safety and/or tolerability measurements.
* Known history of allergy to any component of study intervention.
* History of severe allergic/anaphylactic reaction.
* Pregnancy and/or lactation
* Receipt of any plasma-, protein-, or antibody-based therapeutic agents (e.g., growth hormones or monoclonal antibodies) within 3 months before the first dose of study intervention. Note: Influenza and COVID-19 vaccines will be allowed if administered more than 14 days before the first dose of study intervention.
* Receipt of any investigational agent or treatment within 30 days or 5 half-lives, whichever is longer, before the first dose of study intervention.
* Any active infection, including COVID-19, as determined by the currently applicable standard before study intervention.
* Any acute noninfectious illness within 30 days before day 1.
* Diagnosis of or positive screening result for active COVID-19, hepatitis B surface antigen (HbsAg), hepatitis C virus antibody (HCVAb), or human immunodeficiency virus (HIV)-1 or HIV-2 antibody.
* Unable or unwilling to cooperate with the Investigator for any reason.
* History of any clinically relevant or chronic psychiatric, renal, hepatic, cardiovascular, pancreatic, neurologic, hematologic, or gastrointestinal disease (e.g., inflammatory bowel disease) or current clinically significant liver function test results. Mild anxiety and depression may be acceptable at the investigator's discretion.
* Evidence of any surgical or medical condition that, in the judgment of the Investigator, might interfere with the absorption, distribution, metabolism, or excretion of study intervention. History of cholecystectomy is acceptable.
* Presence of clinically significant electrocardiogram (ECG) finding (confirmed upon repeat testing) that may interfere with any aspect of study conduct or interpretation of results, as follows:

* QT interval corrected for HR according to Fridericia's formula (QTcF) > 450 in males or > 470 msec in females at screening or check-in (day -1).
* Other ECG abnormalities clinically relevant in the judgment of the Investigator.
* Use of any prescription or over-the-counter medications (apart from standard doses of analgesics), herbal products (e.g., St. John's Wort, garlic supplements, milk thistle), topical or inhaled steroids, or supplements/vitamins within 7 days before the first dose of SON-1010 and for the duration of the study, except for those approved by the Investigator and Sponsor (e.g., oral contraceptives, hormone replacement therapy).
* Recent use of systemic steroids within 14 days of enrollment, except for physiologic doses for steroid replacement. Limited doses of systemic steroids (e.g., in patients with exacerbation of reactive airway disease) must have been completed at least 10 days before enrollment.
* Use of biotin (i.e. Vitamin B7) or supplemental biotin higher than the daily adequate intake of 30 µg (FDA 2019). Patients who switch from a high dose to a dose of 30 µg/day or less are eligible.
* History of alcohol or substance abuse within 6 months before the first dose of SON-1010 per the criteria in the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V).
* History of any major surgery within 3 months before the first dose of study intervention.
* Donation or receipt of blood or blood product within 3 months before the first dose of SON-1010 and for the duration of the study.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s


The people analysing the results/data
Intervention assignment
Other
Other design features
Phase
Phase 0
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
27/07/2022
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
17/05/2023
Sample size
Target
Accrual to date
Final
32
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 0 0
Nucleus Network Pty Ltd - Melbourne
Recruitment postcode(s) [1] 0 0
3004 - Melbourne

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Sonnet BioTherapeutics
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Richard Kenney, MD
Address 0 0
Sonnet BioTherapeutics
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.


Results not provided in https://clinicaltrials.gov/study/NCT05408572